BMC Pregnancy and Childbirth (Oct 2024)

Complete blood count as a biomarker for preeclampsia with severe features diagnosis: a machine learning approach

  • Daniella Castro Araújo,
  • Alexandre Afonso de Macedo,
  • Adriano Alonso Veloso,
  • Patricia Nessralla Alpoim,
  • Karina Braga Gomes,
  • Maria das Graças Carvalho,
  • Luci Maria SantAna Dusse

DOI
https://doi.org/10.1186/s12884-024-06821-4
Journal volume & issue
Vol. 24, no. 1
pp. 1 – 13

Abstract

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Abstract Objective This study introduces the complete blood count (CBC), a standard prenatal screening test, as a biomarker for diagnosing preeclampsia with severe features (sPE), employing machine learning models. Methods We used a boosting machine learning model fed with synthetic data generated through a new methodology called DAS (Data Augmentation and Smoothing). Using data from a Brazilian study including 132 pregnant women, we generated 3,552 synthetic samples for model training. To improve interpretability, we also provided a ridge regression model. Results Our boosting model obtained an AUROC of 0.90±0.10, sensitivity of 0.95, and specificity of 0.79 to differentiate sPE and non-PE pregnant women, using CBC parameters of neutrophils count, mean corpuscular hemoglobin (MCH), and the aggregate index of systemic inflammation (AISI). In addition, we provided a ridge regression equation using the same three CBC parameters, which is fully interpretable and achieved an AUROC of 0.79±0.10 to differentiate the both groups. Moreover, we also showed that a monocyte count lower than $$490 /mm^{3}$$ 490 / m m 3 yielded a sensitivity of 0.71 and specificity of 0.72. Conclusion Our study showed that ML-powered CBC could be used as a biomarker for sPE diagnosis support. In addition, we showed that a low monocyte count alone could be an indicator of sPE. Significance Although preeclampsia has been extensively studied, no laboratory biomarker with favorable cost-effectiveness has been proposed. Using artificial intelligence, we proposed to use the CBC, a low-cost, fast, and well-spread blood test, as a biomarker for sPE.

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